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A conditional gene-based association framework integrating isoform-level eQTL data reveals new susceptibility genes for schizophrenia

eLife, 2022-04, Vol.11

2022

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Integrated transcriptomic and regulatory network analyses identify microRNA-200c as a novel repressor of human pluripotent stem cell-derived cardiomyocyte differentiation and maturation

Cardiovascular research, 2018-05, Vol.114 (6), p.894-906

2018

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A fast and accurate SNP detection algorithm for next-generation sequencing data

Nature communications, 2012, Vol.3 (1), p.1258-1258, Article 1258

2012

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Coagulation factors and the incidence of COVID-19 severity: Mendelian randomization analyses and supporting evidence

Signal transduction and targeted therapy, 2021-06, Vol.6 (1), p.222-222, Article 222

2021

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The support of human genetic evidence for approved drug indications

Nature genetics, 2015-08, Vol.47 (8), p.856-860

2015

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Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes

Communications biology, 2020-01, Vol.3 (1), p.6-6, Article 6

2020

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QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes

Nucleic acids research, 2020-01, Vol.48 (D1), p.D983-D991

2020

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QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes

Nucleic acids research, 2023-01, Vol.51 (D1), p.D1122-D1128

2023

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Genome-wide association and functional interrogation identified a variant at 3p26.1 modulating ovarian cancer survival among Chinese women

Cell discovery, 2021-12, Vol.7 (1), p.121-121, Article 121

2021

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GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

Nucleic acids research, 2016-01, Vol.44 (D1), p.D869-D876

2016

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Serine metabolism antagonizes antiviral innate immunity by preventing ATP6V0d2-mediated YAP lysosomal degradation

Cell metabolism, 2021-05, Vol.33 (5), p.971-987.e6

2021

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GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits

Nucleic acids research, 2018-07, Vol.46 (W1), p.W114-W120

2018

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GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications

Nucleic acids research, 2013-07, Vol.41 (Web Server issue), p.W150-W158

2013

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JMJD6 modulates DNA damage response through downregulating H4K16ac independently of its enzymatic activity

Cell death and differentiation, 2020-03, Vol.27 (3), p.1052-1066

2020

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Neurobiological substrates underlying the effect of genomic risk for depression on the conversion of amnestic mild cognitive impairment

Brain (London, England : 1878), 2018-12, Vol.141 (12), p.3457-3471

2018

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GBC: a parallel toolkit based on highly addressable byte-encoding blocks for extremely large-scale genotypes of species

Genome Biology, 2023-04, Vol.24 (1), p.76-76, Article 76

2023

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Hippocampal transcriptome-wide association study and neurobiological pathway analysis for Alzheimer's disease

PLoS genetics, 2021-02, Vol.17 (2), p.e1009363-e1009363

2021

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Editorial: Deciphering Non-Coding Regulatory Variants: Computational and Functional Validation

Frontiers in bioengineering and biotechnology, 2021-11, Vol.9, p.769614-769614

2021

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GWASdb: a database for human genetic variants identified by genome-wide association studies

Nucleic acids research, 2012-01, Vol.40 (Database issue), p.D1047-D1054

2012

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Maternal antibiotic exposure enhances ILC2 activation in neonates via downregulation of IFN1 signaling

Nature communications, 2023-12, Vol.14 (1), p.8332-8332, Article 8332

2023

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regBase: whole genome base-wise aggregation and functional prediction for human non-coding regulatory variants

Nucleic acids research, 2019-12, Vol.47 (21), p.e134-e134

2019

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CHIMGEN: a Chinese imaging genetics cohort to enhance cross-ethnic and cross-geographic brain research

Molecular psychiatry, 2020-03, Vol.25 (3), p.517-529

2020

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Landscape of enhancer disruption and functional screen in melanoma cells

Genome Biology, 2023-10, Vol.24 (1), p.248-32, Article 248

2023

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An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

Nature communications, 2023-03, Vol.14 (1), p.1208-1208, Article 1208

2023

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epiCOLOC: Integrating Large-Scale and Context-Dependent Epigenomics Features for Comprehensive Colocalization Analysis

Frontiers in genetics, 2020-02, Vol.11, p.53-53

2020

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A conditional gene-based association framework integrating isoform-level eQTL data reveals new susceptibility genes for schizophrenia

Integrated transcriptomic and regulatory network analyses identify microRNA-200c as a novel repressor of human pluripotent stem cell-derived cardiomyocyte differentiation and maturation

A fast and accurate SNP detection algorithm for next-generation sequencing data

Coagulation factors and the incidence of COVID-19 severity: Mendelian randomization analyses and supporting evidence

The support of human genetic evidence for approved drug indications

Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes

QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes

QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes

Genome-wide association and functional interrogation identified a variant at 3p26.1 modulating ovarian cancer survival among Chinese women

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

Serine metabolism antagonizes antiviral innate immunity by preventing ATP6V0d2-mediated YAP lysosomal degradation

GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits

GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications

JMJD6 modulates DNA damage response through downregulating H4K16ac independently of its enzymatic activity

Neurobiological substrates underlying the effect of genomic risk for depression on the conversion of amnestic mild cognitive impairment

GBC: a parallel toolkit based on highly addressable byte-encoding blocks for extremely large-scale genotypes of species

Hippocampal transcriptome-wide association study and neurobiological pathway analysis for Alzheimer's disease

Editorial: Deciphering Non-Coding Regulatory Variants: Computational and Functional Validation

GWASdb: a database for human genetic variants identified by genome-wide association studies

Maternal antibiotic exposure enhances ILC2 activation in neonates via downregulation of IFN1 signaling

regBase: whole genome base-wise aggregation and functional prediction for human non-coding regulatory variants

CHIMGEN: a Chinese imaging genetics cohort to enhance cross-ethnic and cross-geographic brain research

Landscape of enhancer disruption and functional screen in melanoma cells

An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

epiCOLOC: Integrating Large-Scale and Context-Dependent Epigenomics Features for Comprehensive Colocalization Analysis

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